# Cylex, Inc. – FDA Inspection, Dec 17, 2008

Source: https://www.keypedia.com/records/fda_inspections/cylex-inc/a4e40955-ab65-469c-a651-ce8b47399166
Source feed: FDA_Inspections

> FDA inspection 552589 of Cylex, Inc., December 17, 2008. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 552589
- Company Name: Cylex, Inc.
- Inspection Date: 2008-12-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 785785 - 2012-06-11

Company: https://www.keypedia.com/companies/cylex-inc/8f0272cf-a5ee-45c0-80d7-4a41e455982e

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7